A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5339n100



Internal ID22791426
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:92632131..92716216hg38UCSC Ensembl
chr4:93553282..93637367hg19UCSC Ensembl
chr4:93772305..93856390hg18UCSC Ensembl
Cytoband4q22.1
Allele length
AssemblyAllele length
hg3884086
hg1984086
hg1884086
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv999973, nsv1014347, nsv1008889
Samples
Known GenesGRID2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv5339n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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